Thinning of the Corpus Callosum and Cerebellar Atrophy is Correlated with Phenotypic Severity in a Family with Spastic Paraplegia Type 11

BACKGROUND: Mutations in the spatacsin gene are associated with spastic paraplegia type 11 (SPG11), which is the most-common cause of autosomal recessive hereditary spastic paraplegia. Although SPG11 has diverse phenotypes, thinning of the corpus callosum is an important feature. CASE REPORT: Clinic...

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Detalles Bibliográficos
Autores principales: Rajakulendran, Sanjeev, Paisán-Ruiz, Coro, Houlden, Henry
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Neurological Association 2011
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131536/
https://www.ncbi.nlm.nih.gov/pubmed/21779300
http://dx.doi.org/10.3988/jcn.2011.7.2.102

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3131536/
https://www.ncbi.nlm.nih.gov/pubmed/21779300
http://dx.doi.org/10.3988/jcn.2011.7.2.102

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